CHMP Adopts Positive Opinion for Aflibercept, Pegfilgrastim Biosimilars:  On January 30, 2025, the European Medicines Agency (EMA) Committee ...

Valneva’s chikungunya vaccine Ixchiq has been greenlit by the UK’s Medicines and Healthcare products Regulatory Agency (MHRA) ...

Exo-Top was established under the jurisdiction of the State of Nevada. Basing Exo-Top in the U.S. offers key advantages, including proximity to strategic partners, access to a robust biopharma ...

State leaders are reviving talk of importing prescription drugs from Canada, even as US drugmakers and health-care attorneys ...

Ms. Fogarty has served at Tonix since 2016, most recently as Executive Vice President, Product DevelopmentTonix is Preparing for Potential Launch ...

The EUR 0.75 co-payment for every prescription in place as of the 1st of January 2025 is not a good solution, says Vice-Dean ...

The ruling requires all trials across the EU to be filed through the European Medicines Agency’s digital filing system.

Recent health news highlights include a review of the safety of Alzheimer's drug Leqembi, legal charges against a New York ...

The European Union’s AI Act has requirements that begin to apply from 2 February 2025 and will have regulatory implications for AI globally. For medicines development, the act will affect AI ...

The commission is a quasi-state agency established by law in 2010 to recruit and oversee lawyers who judges appoint to represent the indigent. They are led by a nine-member commission consisting ...

New CFPB leadership expected to rescind agency guidance Report lays out ways states can bolster consumer finance laws Banks and other companies hoping to escape guidance from the Consumer Financial ...

The number of irregular border crossings into the European Union fell significantly in 2024, according to the bloc’s border control agency Frontex, something which it attributed to intensified ...